Variant report

Variant	nsv997988
Chromosome Location	chr4:122334332-122412234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:122369407-122369765	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:122405814-122405941	HepG2	liver:	n/a	n/a
3	BATF	chr4:122394135-122394406	GM12878	blood:	n/a	n/a
4	BCL3	chr4:122334423-122334652	GM12878	blood:	n/a	n/a
5	BHLHE40	chr4:122405839-122406007	K562	blood:	n/a	n/a
6	BHLHE40	chr4:122405819-122405913	GM12878	blood:	n/a	n/a
7	BRCA1	chr4:122384011-122384012	GM12878	blood:	n/a	n/a
8	CBX3	chr4:122383685-122384304	HCT-116	colon:	n/a	n/a
9	CBX3	chr4:122369301-122369870	HCT-116	colon:	n/a	n/a
10	CBX3	chr4:122398696-122399021	HCT-116	colon:	n/a	n/a
11	CEBPB	chr4:122375401-122375699	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr4:122394598-122394735	H1-hESC	embryonic stem cell:	n/a	chr4:122394694-122394705
13	CEBPB	chr4:122394549-122394862	A549	lung:	n/a	chr4:122394694-122394705
14	CEBPB	chr4:122369204-122369938	HCT-116	colon:	n/a	n/a
15	CEBPB	chr4:122394531-122394871	HepG2	liver:	n/a	chr4:122394694-122394705
16	CEBPB	chr4:122351397-122351423	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:122394540-122394863	IMR90	lung:	n/a	chr4:122394694-122394705
18	CEBPB	chr4:122405886-122405995	HepG2	liver:	n/a	n/a
19	CTCF	chr4:122405820-122405970	SAEC	small airway:	n/a	n/a
20	CTCF	chr4:122405760-122405910	GM12801	blood:	n/a	n/a
21	CTCF	chr4:122383960-122384110	AG09319	gingival:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
22	CTCF	chr4:122342840-122342990	HCT-116	colon:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
23	CTCF	chr4:122405800-122405950	NB4	blood:	n/a	n/a
24	CTCF	chr4:122342880-122343030	HPF	lung:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
25	CTCF	chr4:122383960-122384110	A549	lung:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
26	CTCF	chr4:122386160-122386310	Hela-S3	cervix:	n/a	n/a
27	CTCF	chr4:122383940-122384090	SAEC	small airway:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
28	CTCF	chr4:122405760-122405910	HEK293	kidney:	n/a	n/a
29	CTCF	chr4:122405840-122405990	GM06990	blood:	n/a	n/a
30	CTCF	chr4:122383863-122384154	Lung_OC	lung:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
31	CTCF	chr4:122383580-122383730	K562	blood:	n/a	n/a
32	CTCF	chr4:122342900-122343050	HRE	kidney:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
33	CTCF	chr4:122383620-122384383	SK-N-SH	brain:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
34	CTCF	chr4:122342920-122343070	HCM	heart:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
35	CTCF	chr4:122342860-122343010	AG10803	skin:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
36	CTCF	chr4:122405784-122406057	GM12891	blood:	n/a	n/a
37	CTCF	chr4:122342860-122343010	HCM	heart:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
38	CTCF	chr4:122405800-122405950	A549	lung:	n/a	n/a
39	CTCF	chr4:122383260-122383410	NHDF-neo	bronchial:	n/a	n/a
40	CTCF	chr4:122386200-122386350	GM12867	blood:	n/a	n/a
41	CTCF	chr4:122382624-122382683	Kidney_OC	kidney:	n/a	chr4:122382651-122382660 chr4:122382651-122382664
42	CTCF	chr4:122342860-122343010	HMF	breast:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
43	CTCF	chr4:122342940-122343090	GM12873	blood:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
44	CTCF	chr4:122383940-122384090	AoAF	blood vessel:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
45	CTCF	chr4:122383920-122384070	GM12864	blood:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
46	CTCF	chr4:122405800-122405950	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:122383878-122384137	HepG2	liver:	n/a	chr4:122384011-122384027 chr4:122384012-122384033 chr4:122384010-122384028
48	CTCF	chr4:122383840-122383990	HFF-Myc	foreskin:	n/a	n/a
49	CTCF	chr4:122342940-122343090	RPTEC	kidney:	n/a	chr4:122342943-122342964 chr4:122342949-122342965
50	CTCF	chr4:122405780-122405930	GM12864	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:122376685-122376735	SK-N-SH_RA	brain:	n/a
2	chr4:122376685-122376735	HMEC	breast:	n/a
3	chr4:122376685-122376735	SK-N-SH	brain:	n/a
4	chr4:122376685-122376735	ECC-1	luminal epithelium:	n/a
5	chr4:122376685-122376735	NT2-D1	testis:	n/a
6	chr4:122376685-122376735	BE2_C	brain:	n/a
7	chr4:122376685-122376735	AG04449	skin:	fetal
8	chr4:122376685-122376735	HNPCEpiC	eye:	n/a
9	chr4:122376685-122376735	HRCEpiC	kidney:	n/a
10	chr4:122376685-122376735	RPTEC	kidney:	n/a
11	chr4:122376685-122376735	PrEC	prostate:	n/a
12	chr4:122376685-122376735	K562	blood:	n/a
13	chr4:122376685-122376735	AG09309	skin:	n/a
14	chr4:122376685-122376735	GM19239	blood:	n/a
15	chr4:122376685-122376735	ovcar-3	ovarian:	n/a
16	chr4:122376685-122376735	HEK293	kidney:	embryo
17	chr4:122376685-122376735	AG04450	lung:	fetal
18	chr4:122376685-122376735	NH-A	brain:	n/a
19	chr4:122376685-122376735	MCF-7	breast:	n/a
20	chr4:122376685-122376735	HL-60	blood:	n/a
21	chr4:122376685-122376735	HPAEpiC	pulmonary alveolar:	n/a
22	chr4:122376685-122376735	Caco-2	colon:	n/a
23	chr4:122376685-122376735	HUVEC	blood vessel:	n/a
24	chr4:122376685-122376735	HCF	heart:	n/a
25	chr4:122376685-122376735	SAEC	small airway:	n/a
26	chr4:122376685-122376735	HCM	heart:	n/a
27	chr4:122376685-122376735	NHBE	bronchial:	n/a
28	chr4:122376685-122376735	AG09319	gingival:	n/a
29	chr4:122376685-122376735	SKMC	muscle:	n/a
30	chr4:122376685-122376735	IMR90	lung:	fetal
31	chr4:122376685-122376735	HepG2	liver:	n/a
32	chr4:122376685-122376735	T-47D	breast:	n/a
33	chr4:122376685-122376735	NB4	blood:	n/a
34	chr4:122376685-122376735	MCF10A-Er-Src	breast:	n/a
35	chr4:122376685-122376735	CMK	blood:	n/a
36	chr4:122376685-122376735	A549	lung:	n/a
37	chr4:122376685-122376735	GM12878	blood:	n/a
38	chr4:122376685-122376735	GM06990	blood:	n/a
39	chr4:122376685-122376735	HAEpiC	amniotic membrane:	n/a
40	chr4:122376685-122376735	SK-N-MC	brain:	n/a
41	chr4:122376685-122376735	GM12892	blood:	n/a
42	chr4:122376685-122376735	Hepatocyte	liver:	n/a
43	chr4:122376685-122376735	H1-hESC	embryonic stem cell:	embryo
44	chr4:122376685-122376735	Hela-S3	cervix:	n/a
45	chr4:122376685-122376735	HCT-116	colon:	n/a
46	chr4:122376685-122376735	AG10803	skin:	n/a
47	chr4:122376685-122376735	NHDF-neo	bronchial:	n/a
48	chr4:122376685-122376735	HRE	kidney:	n/a
49	chr4:122376685-122376735	HCPEpiC	choroid plexus:	n/a
50	chr4:122376685-122376735	U87	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:122390684..122392219-chr4:122410927..122413477,2	K562	blood:
2	chr4:122390684..122392219-chr4:122410927..122413477,2	K562	blood:
3	chr4:122291624..122292430-chr4:122342879..122343479,3	MCF-7	breast:
4	chr4:122383962..122386021-chr4:122397166..122399393,2	K562	blood:
5	chr4:122383570..122384412-chr6:100888804..100889304,2	MCF-7	breast:
6	chr4:122383962..122386021-chr4:122397166..122399393,2	K562	blood:
7	chr4:122379568..122382631-chr4:122383920..122387075,3	K562	blood:
8	chr4:122198494..122199456-chr4:122342475..122343364,3	MCF-7	breast:
9	chr4:122383589..122384125-chr4:122456174..122457010,2	MCF-7	breast:
10	chr4:122405367..122406326-chr4:122657740..122658516,2	K562	blood:
11	chr4:122406611..122408382-chr4:122588415..122590741,2	K562	blood:
12	chr4:122379568..122382631-chr4:122383920..122387075,3	K562	blood:
13	chr4:122383988..122384720-chr4:122555173..122555707,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC079341.1-1	chr4:122411144-122411200	XLOC_003675
2	lnc-AC079341.1-7	chr4:122372696-122373122	NONHSAT098142

Variant related genes	Relation type
TUBB4BP5	TF binding region
TUBB4BP5	CpG island

Extended variants
information (count: 1523 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1523 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs575958798	chr4:122339424-122339425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570995958	chr4:122339439-122339440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs544797634	chr4:122339540-122339541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564973507	chr4:122339568-122339569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs144920951	chr4:122339577-122339578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs567855601	chr4:122339618-122339619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547606809	chr4:122339653-122339654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183827538	chr4:122339655-122339656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs72919700	chr4:122339662-122339663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140450166	chr4:122339720-122339721	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs1606575	chr4:122339739-122339740	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs538210725	chr4:122339757-122339758	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs79670834	chr4:122339797-122339798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188041385	chr4:122339807-122339808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534167545	chr4:122339808-122339809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs553949708	chr4:122339812-122339813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs374882204	chr4:122339836-122339837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs573856951	chr4:122339905-122339906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145259703	chr4:122339906-122339907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs556412417	chr4:122339917-122339918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs575984000	chr4:122339922-122339923	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs544977118	chr4:122339935-122339936	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572131348	chr4:122339966-122339967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs34355403	chr4:122340003-122340004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs12651280	chr4:122340005-122340006	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs115049447	chr4:122340014-122340015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs541079772	chr4:122340040-122340041	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561071134	chr4:122340088-122340089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs190560946	chr4:122340143-122340144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs141285917	chr4:122340164-122340165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs11098617	chr4:122340165-122340166	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs183117509	chr4:122340189-122340190	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531642367	chr4:122340212-122340213	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551741935	chr4:122340221-122340222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs11733024	chr4:122340224-122340225	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs577370248	chr4:122340234-122340235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs369389825	chr4:122340255-122340256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs79973681	chr4:122340262-122340263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs535283762	chr4:122340276-122340277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567542959	chr4:122340282-122340283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs60715033	chr4:122340374-122340375	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs556620755	chr4:122340377-122340378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs13353588	chr4:122340387-122340388	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs28513945	chr4:122349876-122349877	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs78987177	chr4:122349879-122349880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs13132003	chr4:122349897-122349898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs559829959	chr4:122350015-122350016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs28461852	chr4:122350016-122350017	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs59363516	chr4:122350031-122350032	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs28600811	chr4:122350043-122350044	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
small cell lung cancer	20016488	CNVD
Clear cell renal cell carcinoma	18791270	CNVD
Acute myeloid leukemia	19651601	CNVD
Gastric cancer	16891809	CNVD
Olfactory neuroblastoma	18408657	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:102 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:122339400-122340400	Enhancers	Left Ventricle	heart
2	chr4:122349800-122350600	Enhancers	Muscle Satellite Cultured Cells	--
3	chr4:122349800-122350800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr4:122349800-122351000	Enhancers	Hela-S3	cervix
5	chr4:122350000-122350400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr4:122350000-122350400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr4:122350000-122350400	Enhancers	NH-A	brain
8	chr4:122350000-122350600	Enhancers	HMEC	breast
9	chr4:122350000-122350800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:122350200-122350800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:122360400-122361200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr4:122360600-122361000	ZNF genes & repeats	Pancreas	Pancrea
13	chr4:122360600-122361200	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:122360600-122361200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr4:122360600-122361200	ZNF genes & repeats	Gastric	stomach
16	chr4:122360600-122361200	Enhancers	Right Ventricle	heart
17	chr4:122360600-122361400	ZNF genes & repeats	Spleen	Spleen
18	chr4:122360800-122361200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr4:122361000-122361200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr4:122361200-122372600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr4:122368400-122369600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr4:122369000-122370000	Enhancers	Fetal Intestine Small	intestine
23	chr4:122369000-122370000	Enhancers	Stomach Mucosa	stomach
24	chr4:122369200-122369800	Enhancers	HepG2	liver
25	chr4:122370000-122375600	Weak transcription	Stomach Mucosa	stomach
26	chr4:122370400-122371200	Enhancers	Fetal Kidney	kidney
27	chr4:122372600-122373000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:122372600-122373000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:122373000-122375800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
30	chr4:122374000-122374200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr4:122374200-122374400	Enhancers	Fetal Lung	lung
32	chr4:122374200-122375400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr4:122374600-122375600	Weak transcription	Fetal Lung	lung
34	chr4:122375000-122376800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
35	chr4:122375400-122376600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr4:122375400-122376600	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr4:122375400-122376600	Enhancers	HUES6 Cell Line	embryonic stem cell
38	chr4:122375600-122376000	Enhancers	Left Ventricle	heart
39	chr4:122375600-122376000	Enhancers	Stomach Mucosa	stomach
40	chr4:122375600-122376000	Enhancers	Hela-S3	cervix
41	chr4:122375600-122376200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr4:122375600-122376200	Enhancers	Fetal Lung	lung
43	chr4:122375600-122376600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr4:122375600-122376600	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr4:122375600-122376600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chr4:122375600-122376600	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr4:122375600-122376800	Enhancers	H1 Cell Line	embryonic stem cell
48	chr4:122375800-122376000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:122375800-122376000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr4:122375800-122376200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell

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